心肌梗死患者心脏特异性整合蛋白的诊断和预后价值

R. R. Heirullin, V. Ruzov, M. V. Frolova
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Over the course of 18 months, clinical outcomes were recorded for participants: a composite endpoint of death due to cardiac causes, incident ADHF, worsening TSH results, and intensification of pharmacotherapy.Results. In patients with a history of HF, the level of cBIN-1(CS) in the blood was 0.871 ng/ml, in the group with risk factors for HF – 0.690 ng/ml. The results of TSH on day 7 are associated with an increase in cBIN-1(CS) content and a decrease in the result by 80.45 m in the STEMI group and by 177.36 m in the NSTEMI group (p = 0.002). ROC-analysis of the probability of a fatal outcome based on the cBIN-1(CS) level showed the area under the ROC curve in subgroup I with an established diagnosis of HF of 0.743 ± 0.098 (p = 0.023), in subgroup II – 0.746 ± 0.146 (p = 0.103). ROC-analysis of the probability of achieving the composite endpoint for each of the patient subgroups showed AUC of 0.859 ± 0.058 and 0.751 ± 0.063 (p < 0.001), respectively. 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摘要

简介评估新的生物标志物 cBIN-1(CS)具有优势;其浓度与钠尿肽不同,不依赖于血容量状态、体重和慢性肾脏病,这在高血压诊断中似乎很有价值。研究血清 cBIN-1(CS)对心肌梗死患者的诊断和预后价值。研究分析了心肌梗死后第 7 天 100 名患者的临床、实验室和仪器数据。子组 I 包括有心房颤动病史的患者,子组 II 包括有心房颤动危险因素的患者。研究包括超声心动图、促甲状腺激素、cBIN-1(CS)测定。在18个月的时间里,对参与者的临床结果进行了记录:心脏原因导致的死亡、ADHF事件、TSH结果恶化以及药物治疗的加强等综合终点。有高血压病史的患者血液中 cBIN-1(CS)的水平为 0.871 纳克/毫升,有高血压危险因素的患者血液中 cBIN-1(CS) 的水平为 0.690 纳克/毫升。第 7 天 TSH 的结果与 cBIN-1(CS)含量的增加有关,STEMI 组的结果降低了 80.45 m,NSTEMI 组降低了 177.36 m(p = 0.002)。基于 cBIN-1(CS)水平的致命结果概率 ROC 分析显示,在已确诊为 HF 的 I 亚组中,ROC 曲线下面积为 0.743 ± 0.098(p = 0.023);在 II 亚组中,ROC 曲线下面积为 0.746 ± 0.146(p = 0.103)。对每个患者亚组达到复合终点的概率进行的 ROC 分析显示,AUC 分别为 0.859 ± 0.058 和 0.751 ± 0.063(p < 0.001)。cBIN-1(CS) 值≥ 0/826 ng/ml(敏感性 80.0%,特异性 70.6%)可被视为心肌梗死后不利预后的标志物。根据心肌梗死后患者的 Kaplan-Meier 生存曲线,cBIN-1(CS)的临界值为 0.826 ng/ml(p < 0.0001),该值被认为是将患者分为不良预后高风险和低风险的最佳值。cBIN-1(CS)生物标志物具有较高的灵敏度和特异性,可作为评估心肌梗死后心肌储备的标志物来预测不良事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic and prognostic value of cardiospecific integrator protein in patients after myocardial infarction
Introduction. Evaluation of the new biomarker cBIN-1(CS) has advantages; its concentration does not depend on volume status, body weight, CKD, in contrast to natriuretic peptides, which seems valuable in the diagnosis of HF.Aim. To study the diagnostic and prognostic value of serum cBIN-1(CS) in patients who have suffered myocardial infarction.Materials and methods. The study analyzed clinical, laboratory and instrumental data of 100 patients on the 7th day after myocardial infarction. Subgroup I included patients with a history of HF, subgroup II included patients with risk factors for developing HF. Studies included echocardiography, TSH, cBIN-1(CS) determination. Over the course of 18 months, clinical outcomes were recorded for participants: a composite endpoint of death due to cardiac causes, incident ADHF, worsening TSH results, and intensification of pharmacotherapy.Results. In patients with a history of HF, the level of cBIN-1(CS) in the blood was 0.871 ng/ml, in the group with risk factors for HF – 0.690 ng/ml. The results of TSH on day 7 are associated with an increase in cBIN-1(CS) content and a decrease in the result by 80.45 m in the STEMI group and by 177.36 m in the NSTEMI group (p = 0.002). ROC-analysis of the probability of a fatal outcome based on the cBIN-1(CS) level showed the area under the ROC curve in subgroup I with an established diagnosis of HF of 0.743 ± 0.098 (p = 0.023), in subgroup II – 0.746 ± 0.146 (p = 0.103). ROC-analysis of the probability of achieving the composite endpoint for each of the patient subgroups showed AUC of 0.859 ± 0.058 and 0.751 ± 0.063 (p < 0.001), respectively. The cBIN-1(CS) value ≥ 0/826 ng/ml (sensitivity 80.0%, specificity 70.6%) can be considered as a marker of unfavorable outcome after myocardial infarction. According to the Kaplan-Meier survival curve for patients after MI, the cut-off value for cBIN-1(CS) is 0.826 ng/ml (p < 0.0001), which was determined to be the most optimal for separating patients into high and low risk of an adverse outcome.Conclusion. The cBIN-1(CS) biomarker has high sensitivity and specificity and can be used as a marker for assessing myocardial reserve after myocardial infarction to predict adverse events.
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